6857-12-1 Usage
Chemical structure
Consists of a morpholine ring attached to the isoindole-1,3-dione structure.
Versatility
Has potential applications in various fields such as pharmaceuticals, agrochemicals, and materials science.
Unique properties
Presence of the morpholine group provides the molecule with the ability to form hydrogen bonds and interact with biological systems.
Potential use as a building block
Can be used for the synthesis of new drug candidates and other bioactive molecules.
Further research and development
Could lead to the discovery of novel compounds with valuable applications in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6857-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6857-12:
(6*6)+(5*8)+(4*5)+(3*7)+(2*1)+(1*2)=121
121 % 10 = 1
So 6857-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O3/c16-12-10-3-1-2-4-11(10)13(17)15(12)9-14-5-7-18-8-6-14/h1-4H,5-9H2
6857-12-1Relevant articles and documents
HYDROXY-, ALKOXY-, AMINOMETHYLATION OF NH-OXAZIRIDINES
Varlamov, S. V.,Kadorkina, G. K.,Kostyanovskii, R. G.
, p. 320 - 325 (2007/10/02)
3,3-Dimethyloxaziridine reacts with chloral and acetaldehyde to give crystalline N-(α-hydroxyalkyl)oxaziridines; the reaction with acetaldehyde is reversible.The N-aminomethylation of NH-oxaziridines is not realized, evidently because of the tendency of oxaziridines to iminate nucleophiles.The weakly nucleophilic chloromethylphthalimide and chloromethyl methyl ether give imidomethyl- and methoxymethyloxaziridines. 3,3-Dimethyldiaziridine reacts with excess chloromethyl methyl eter to give the N-monomethoxymethyl derivative.It is shown that α-hydroxyalkyloxaziridines and methoxymethyl-substituted oxaziridine and dizaridine do not enter into the aminomethylation of compounds with a labile hydrogen.
